Distinct regulatory elements mediate similar expression patterns in the excretory cell of Caenorhabditis elegans

J Biol Chem. 2005 Nov 18;280(46):38787-94. doi: 10.1074/jbc.M505701200. Epub 2005 Sep 13.

Abstract

Identification of cis-regulatory elements and their binding proteins constitutes an important part of understanding gene function and regulation. It is well accepted that co-expressed genes tend to share transcriptional elements. However, recent findings indicate that co-expression data show poor correlation with co-regulation data even in unicellular yeast. This motivates us to experimentally explore whether it is possible that co-expressed genes are subject to differential regulatory control using the excretory cell of Caenorhabditis elegans as an example. Excretory cell is a functional equivalent of human kidney. Transcriptional regulation of gene expression in the cell is largely unknown. We isolated a 10-bp excretory cell-specific cis-element, Ex-1, from a pgp-12 promoter. The significance of the element has been demonstrated by its capacity of converting an intestine-specific promoter into an excretory cell-specific one. We also isolated a cDNA encoding an Ex-1 binding transcription factor, DCP-66, using a yeast one-hybrid screen. Role of the factor in regulation of pgp-12 expression has been demonstrated both in vitro and in vivo. Search for occurrence of Ex-1 reveals that only a small portion of excretory cell-specific promoters contain Ex-1. Two other distinct cis-elements isolated from two different promoters can also dictate the excretory cell-specific expression but are independent of regulation by DCP-66. The results indicate that distinct regulatory elements are able to mediate the similar expression patterns.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP Binding Cassette Transporter, Subfamily B / genetics*
  • Animals
  • Base Sequence
  • Caenorhabditis elegans
  • Caenorhabditis elegans Proteins / chemistry*
  • Caenorhabditis elegans Proteins / genetics
  • Computational Biology
  • DNA / chemistry
  • DNA / metabolism
  • DNA, Complementary / metabolism
  • Gene Deletion
  • Gene Expression Regulation
  • Genes, Reporter
  • Genotype
  • Green Fluorescent Proteins / metabolism
  • Models, Biological
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Promoter Regions, Genetic
  • Protein Binding
  • Protein Structure, Tertiary
  • RNA Interference
  • Transcription Factors / genetics*
  • Transcription, Genetic*
  • Transgenes
  • Two-Hybrid System Techniques

Substances

  • ATP Binding Cassette Transporter, Subfamily B
  • Caenorhabditis elegans Proteins
  • DCP-66 protein, C elegans
  • DNA, Complementary
  • Pgp-12 protein, C elegans
  • Transcription Factors
  • Green Fluorescent Proteins
  • DNA